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Creutzfeldt–Jakob disease (CJD), also known as subacute spongiform encephalopathy or neurocognitive disorder due to prion disease, is a fatal neurodegenerative disease. [ 4 ] [ 1 ] Early symptoms include memory problems, behavioral changes, poor coordination, and visual disturbances. [ 4 ]
CJD (Christliches Jugenddorfwerk Deutschlands) is a German Christian nonprofit organization. [1] The organization was founded in 1947 [ 1 ] by Christian pastor Arnold Dannenmann. CJD is an organisation that deals with youth, education and social work. [ 1 ]
Fatal insomnia is an extremely rare neurodegenerative prion disease that results in trouble sleeping as its hallmark symptom. [2] The majority of cases are familial (fatal familial insomnia [FFI]), stemming from a mutation in the PRNP gene, with the remainder of cases occurring sporadically (sporadic fatal insomnia [sFI]).
The Creutzfeldt-Jakob Disease Surveillance System (CJDSS) is a unit of the Public Health Agency of Canada. It studies the various variants of Creutzfeldt-Jakob Disease , and at least as of 2017, assisted "with DNA sequencing , autopsy and case confirmation". [ 1 ]
vCJD is a separate condition from classic Creutzfeldt–Jakob disease (though both are caused by PrP prions). [9] Both classic and variant CJD are subtypes of Creutzfeldt–Jakob disease. There are three main categories of CJD disease: sporadic CJD, hereditary CJD, and acquired CJD, with variant CJD being in the acquired group along with ...
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Creutzfeldt–Jakob disease, a fatal degenerative brain disorder caused by prions involving the cerebral cortex, the basal ganglia and the spinal cord.; Adrenoleukodystrophy, a rare demyelination disorder also known as Siemerling-Creutzfeldt disease that causes damage to the myelin sheaths of neurons in the brain, resulting in seizures and hyperactivity.